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Davol, Inc., Subs. C. R. Bard, Inc. recalls Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 cm x 25.4 cm) Product Code 5954810. The Bard Ventralight ST Mes
Recalled September 26, 2012 · FDA recall Z-2412-2012 · Davol, Inc., Subs. C. R. Bard
Hazard
Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh product and the 7" x 9" package contains 8" x 10" VENTRALIGHT ST Mesh product · FDA Class II
Units
49 units
Sold at
Nationwide Distribution.
Description
Mislabeled: The 8" x 10" package contains 7" x 9" VENTRALIGHT ST Mesh product and the 7" x 9" package contains 8" x 10" VENTRALIGHT ST Mesh product
Product
Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 cm x 25.4 cm) Product Code 5954810. The Bard Ventralight ST Mesh is a dual-component (absorbable and nonabsorbable) sterile prosthesis. The device classification name is "Mesh, Surgical, Polymeric." It is in tented for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias.
Manufacturer(s)
Davol, Inc., Subs. C. R. Bard, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →